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rs137852240

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137852240(C;T)
Make rs137852240(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139551217
GeneF9
is asnp
is mentioned by
dbSNPrs137852240
ebirs137852240
HLIrs137852240
Exacrs137852240
Varsomers137852240
Maprs137852240
PheGenIrs137852240
hapmaprs137852240
1000 genomesrs137852240
hgdprs137852240
ensemblrs137852240
gopubmedrs137852240
geneviewrs137852240
scholarrs137852240
googlers137852240
pharmgkbrs137852240
gwascentralrs137852240
openSNPrs137852240
23andMers137852240
23andMe allrs137852240
SNP Nexus

SNPshotrs137852240
SNPdbers137852240
MSV3drs137852240
GWAS Ctlgrs137852240
Max Magnitude0
OMIM300746
Desc
Variant0030
Relatedalso
ClinVar
Risk rs137852240(T;T)
Alt rs137852240(T;T)
Reference rs137852240(C;C)
Significance Pathogenic
Disease Hereditary factor IX deficiency disease
Variation info
Gene F9
CLNDBN Hereditary factor IX deficiency disease
Reversed 0
HGVS NC_000023.10:g.138633376C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011336.5,